par Van Bogaert, Patrick 
;Aeby, Alec ;de Borchgrave d'Alténa, Valérie;De Cocq, C;Deprez, M;De Tiege, Xavier ;De Tourtchaninoff, Marianne;Dubru, J M;Foulon, Martine ;Ghariani, S;Grisar, T;Legros, Benjamin ;Ossemann, M;Tugendhaft, P;van Rijckevorsel, Kenou;Verheulpen, Denis ;Groupe de travail des centres francophones de référence de l'epilepsie réfractaire,
Référence Acta neurologica belgica, 106, 2, page (52-60)
Publication Publié, 2006-06
;Aeby, Alec ;de Borchgrave d'Alténa, Valérie;De Cocq, C;Deprez, M;De Tiege, Xavier ;De Tourtchaninoff, Marianne;Dubru, J M;Foulon, Martine ;Ghariani, S;Grisar, T;Legros, Benjamin ;Ossemann, M;Tugendhaft, P;van Rijckevorsel, Kenou;Verheulpen, Denis ;Groupe de travail des centres francophones de référence de l'epilepsie réfractaire, Référence Acta neurologica belgica, 106, 2, page (52-60)
Publication Publié, 2006-06
Article révisé par les pairs
| Résumé : | The authors propose to define the epileptic syndromes with continuous spikes and waves during slow sleep (CSWS) as a cognitive or behavioral impairment acquired during childhood, associated with a strong activation of the interictal epileptiform discharges during NREM sleep--whatever focal or generalized--and not related to another factor than the presence of CSWS. The type of syndrome will be defined according to the neurological and neuropsychological deficit. These syndromes have to be classified among the localization-related epileptic syndromes. Some cases are idiopathic and others are symptomatic. Guidelines for work-up and treatment are proposed. |
